ENST00000651671.1:c.6417C>T
MANE Select
|
ENSP00000498587.1:p.Leu2139=
|
|
ENST00000679595.1:c.*1457C>T
|
ENSP00000506241.1:n.*1457C>T
|
|
ENST00000679969.1:n.3013C>T
|
|
|
ENST00000680003.1:n.2749C>T
|
|
|
ENST00000680133.1:c.6303C>T
|
ENSP00000505319.1:p.Leu2101=
|
|
ENST00000680218.1:c.6297C>T
|
ENSP00000505339.1:p.Leu2099=
|
|
ENST00000680668.1:c.6303C>T
|
ENSP00000506336.1:p.Leu2101=
|
|
ENST00000680778.1:c.4014C>T
|
ENSP00000506033.1:p.Leu1338=
|
|
ENST00000680924.1:c.*3817C>T
|
ENSP00000506031.1:n.*3817C>T
|
|
ENST00000681135.1:c.*4026C>T
|
ENSP00000506636.1:n.*4026C>T
|
|
ENST00000681298.1:n.4522C>T
|
|
|
ENST00000681454.1:c.*5653C>T
|
ENSP00000505763.1:n.*5653C>T
|
|
ENST00000277541.6:c.6417C>T
|
ENSP00000277541.6:p.Leu2139=
|
|
NM_017617.3:c.6417C>T
|
NP_060087.3:p.Leu2139=
|
|
XM_011518717.1:c.5718C>T
|
XP_011517019.1:p.Leu1906=
|
|
NM_017617.5:c.6417C>T
MANE Select
|
NP_060087.3:p.Leu2139=
|
|
XM_011518717.2:c.5694C>T
|
XP_011517019.2:p.Leu1898=
|
|